Product Recalls in Utah

Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,666 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,666 in last 12 months

Showing 481500 of 49,677 recalls

Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Philips has identified that in a limited number of impacted systems the drip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· LEASEIR TECHNOLOGIES SLU

Recalled Item: Brand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number:...

The Issue: The console label for affected devices is missing the "DANGER" symbol.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· Immunotech A.S.

Recalled Item: Estrone RIA Recalled by Immunotech A.S. Due to The affected Estrone RIA kit...

The Issue: The affected Estrone RIA kit lots may rarely give falsely high patient...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Plum Duo Infusion Pump Recalled by ICU Medical, Inc. Due to Plum...

The Issue: Plum Solo and Duo Infusion pumps include a feature, that when selected,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Plum Duo Precision IV Pump Recalled by ICU Medical, Inc. Due to...

The Issue: Plum Solo and Duo Infusion pumps include a feature, that when selected,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Philips has identified that in a limited number of impacted systems the drip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Philips has identified that in a limited number of impacted systems the drip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Philips has identified that in a limited number of impacted systems the drip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Philips has identified that in a limited number of impacted systems the drip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Philips has identified that in a limited number of impacted systems the drip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 15, 2025· NOVADOZ PHARMACEUTICALS LLC

Recalled Item: Glycopyrrolate Oral Solution Recalled by NOVADOZ PHARMACEUTICALS LLC Due to...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 15, 2025· SunMed Holdings, LLC

Recalled Item: Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape...

The Issue: Product contains potentially harmful dosing errors for Vecuronium,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2025· SunMed Holdings, LLC

Recalled Item: Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape...

The Issue: Product contains potentially harmful dosing errors for Vecuronium,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2025· Sysmex America, Inc.

Recalled Item: TS-10/TS-10H Tube Sorter Recalled by Sysmex America, Inc. Due to Under...

The Issue: Under specific conditions, the lift's electromagnetic holding force may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· Diagnostica Stago, Inc.

Recalled Item: Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is...

The Issue: Potential for defect for Asserachrom HPIA lot 271288, which can affect every...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Philips has identified that in a limited number of impacted systems the drip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodDecember 13, 2025· Tom Bumble LLC

Recalled Item: Tom Bumble Nutty Peanut Butter Flake Candy with Peanut & Recalled by Tom...

The Issue: Foreign material.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) RR-GYN LAPAROSCOPY...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) PACER / Recalled...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Elekta, Inc.

Recalled Item: Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment...

The Issue: Due to an error when defining a new stereotactic that users fail to first...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing